Clinical Trial Crossword Challenge!

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Across
  1. 1. Electronic capture of subject level data
  2. 4. To confirm source CRF entries match original source records
  3. 6. Governing document for study conduct
  4. 9. Summarizes all known clinical and nonclinical data about the IP
  5. 10. Primary or secondary outcomes
Down
  1. 2. To assign subjects by chance
  2. 3. Reviews and approves research to ensure participant safety and ethical conduct
  3. 5. Blinding helps prevents this in clinical trials
  4. 7. Study phase that focuses on safety, tolerability, and dose-finding in a small group of healthy participants
  5. 8. Outlines how statistical analysis will be performed
  6. 11. Group that oversees participant safety and trial integrity